Goat Anti-Mouse IgG (H+L) Secondary Antibody, Unconjugated

SKU:BHA21012535
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Overview
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Goat anti-Mouse IgG (H+L) secondary antibody (Polyclonal). Designed to recognize Mouse immunoglobulins in indirect detection formats. Commonly used as a detection reagent in immunoassays where secondary specificity and label choice matter.
Target Mouse IgG (H+L)
Host Goat
Reactivity Mouse
Options selector
Catalog no. Size
BA1038-1mg 1 mg
BA1038-5mg 5 mg
Available Options

Select the variant that best fits your experiment. Availability and lead time may vary by option.

  • Options:
    • 1 mg; 5 mg
  • Lead time: typically ships in ~2–3 business days; timing may vary by selected option.
  • Storage: At -20℃ for one year from date of receipt. Avoid repeated freezing and thawing.
  • Shipping: cold-chain shipment (typically with ice packs).
  • Upon receipt: store at the recommended temperature as soon as possible; avoid repeated freeze-thaw cycles.
  • Sales terms and conditions: Please review prior to ordering.
Field Specification
Mfr No BA1038
Clonality
  • Polyclonal
Host Goat
Immunogen Mouse IgG (whole molecule).
Product Type
  • Antibodies
  • Secondary Antibodies
Reactivity
  • Mouse
Storage At -20℃ for one year from date of receipt. Avoid repeated freezing and thawing.
Target Mouse IgG (H+L)

Overview

Goat Anti-Mouse IgG (H+L) Secondary Antibody, Unconjugated is a secondary antibody used for indirect detection of primary antibodies and immunoglobulins from Mouse IgG (H+L). It is commonly selected for experiments where label choice and species/isotype recognition affect signal interpretation.

Key elements and design rationale

  • Host species: Goat (antibody source species).
  • Recognition: Designed to recognize immunoglobulins from Mouse IgG (H+L) for secondary detection.
  • Clonality: Polyclonal.
  • Specificity notes (provided): This antibody is specific for mouse IgG and shows no cross-reactivity with human/bovine/rabbit IgG..

unconjugated Goat Anti-mouse IgG (H+L) secondary antibody This antibody is specific for mouse IgG and shows no cross-reactivity with human/bovine/rabbit IgG.

Background (provided): Secondary antibodies offer increased versatility enabling users to use many detection systems such as HRP, AP and fluorescence. They can also provide greater sensitivity through signal amplification as multiple secondary antibodies can bind to a single primary antibody, and secondary antibodies' FC regions provide further binding locations for biotin, enable the use of ABC and SABC to further amplify the signal. Most commonly, secondary antibodies are generated by immunizing the host animal with a pooled population of immunoglobulins from the target species. They are then purified through immunoaffinity chromatography and modified with antibody fragmentation, label conjugation, etc., to generate highly specific reagents.

Biological background

Secondary antibodies enable indirect detection by binding to the constant regions of primary antibodies. Fragment specificity matters: reagents labeled as (H+L) recognize epitopes on both heavy and light chains of the target-species immunoglobulin, while Fc- or light-chain-specific secondaries can reduce off-target signal in some multiplex or isotype-specific designs. Label choice (fluorophore, enzyme, biotin) affects sensitivity, multiplex compatibility, and how signal should be interpreted across sample types.

Research relevance and current trends

  • Multiplex imaging and spatial biology workflows increasingly rely on well-matched secondary antibodies to minimize cross-reactivity between species and isotypes.
  • Biotin–streptavidin amplification remains common for tissue staining and low-abundance targets, with controls used to monitor endogenous biotin background where relevant.
  • Quantitative immunoassays often combine consistent secondary reagents with standardized detection chemistries to support cross-experiment comparability.

Common research applications

  • Western blotting: enables indirect detection of primary antibodies bound to target proteins after gel separation.
  • Immunohistochemistry/Immunofluorescence: supports localization and comparative staining in cells or tissue sections.
  • ELISA and plate-based assays: provides high-throughput readouts for binding and detection.

Notes for experimental interpretation

  • Cross-reactivity and background: non-target binding can arise from endogenous immunoglobulins, closely related species, or multiplexed primary antibodies. Species selection and cross-adsorption (when specified) help reduce unwanted signal.
  • Control concepts: no-primary controls, isotype controls, and orthogonal detection channels help distinguish specific staining from background. For biotin-based systems, consider controls for endogenous biotin where relevant.

Customization & Add-ons: Can’t find the antibody you need—or require a custom format for your assay? We can help you source the best match or support custom antibody solutions for diverse research needs, including species and isotype selection, conjugations and labeling (e.g., HRP/AP, biotin, fluorophores), purification grade options (Protein A/G, affinity purified), formulation preferences (buffer selection, carrier-free, glycerol-free), custom concentrations and aliquoting, low-endotoxin options for cell-based work, and application-focused QC/validation support (project dependent). Click Talk to a Scientist to submit a request, email us at support@biohippo.com, or explore our Research Services for additional support—our team will follow up with feasibility details and next steps.

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Experience the power of Celltrypse™, c-LEcta's innovative enzyme solution for gentle and efficient cell dissociation. Request your free sample and discover a superior alternative for your cell culture workflows.

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